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慢性阻塞性肺疾病患者肺动脉压的长期病程

Long-term course of pulmonary arterial pressure in chronic obstructive pulmonary disease.

作者信息

Weitzenblum E, Sautegeau A, Ehrhart M, Mammosser M, Hirth C, Roegel E

出版信息

Am Rev Respir Dis. 1984 Dec;130(6):993-8. doi: 10.1164/arrd.1984.130.6.993.

Abstract

Ninety-three patients with severe chronic obstructive pulmonary disease (COPD) of the bronchitic (n = 74) or emphysematous type (n = 19), who all had arterial hypoxemia, underwent 2 right cardiac catheterizations in a clinical steady state, with a delay of 5 yr or more between the first and the last catheterization. No patients received long-term O2 therapy or pulmonary vasodilator drugs. Patients were divided into 2 groups according to the initial level of mean pulmonary artery pressure (Pap). Group 1 included 61 patients without initial pulmonary arterial hypertension (PAH), Pap being less than 20 mmHg; the average delay between the 2 catheterizations was 93.4 +/- 26.8 months. Group 2 included 32 patients with initial PAH (Pap greater than or equal to 20 mmHg), and the average delay was 85.0 +/- 26.0 months. The changes in Pap were small. They ranged from 15.5 +/- 2.4 to 19.6 +/- 7.0 mmHg in Group 1 (p less than 0.001) and from 25.8 +/- 5.6 to 27.8 +/- 9.5 mmHg in Group 2 (NS). The average increase in Pap was 0.65 mmHg/yr in Group 1 and 0.39 mmHg/yr in Group 2 (no statistical difference between the 2 groups). The other hemodynamic parameters (pulmonary capillary wedge pressure, right ventricle filling pressure, cardiac output) did not change. Hemodynamic "worsening," which was defined by an increase in Pap by greater than or equal to 5 mm Hg, was observed in 29% of the patients (n = 27). In these patients, there was a marked worsening of hypoxemia, which was not observed in the remaining 66 patients.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

93例患有支气管型(n = 74)或肺气肿型(n = 19)严重慢性阻塞性肺疾病(COPD)且均有动脉血氧不足的患者,在临床稳定状态下接受了两次右心导管检查,首次与末次导管检查间隔时间为5年或更长时间。无患者接受长期氧疗或肺血管扩张药物治疗。根据平均肺动脉压(Pap)的初始水平将患者分为两组。第1组包括61例无初始肺动脉高压(PAH)的患者,Pap小于20 mmHg;两次导管检查之间的平均间隔时间为93.4±26.8个月。第2组包括32例初始患有PAH(Pap大于或等于20 mmHg)的患者,平均间隔时间为85.0±26.0个月。Pap的变化很小。第1组中Pap从15.5±2.4 mmHg变化至19.6±7.0 mmHg(p < 0.001),第2组中从25.8±5.6 mmHg变化至27.8±9.5 mmHg(无统计学差异)。第1组中Pap的平均年增加值为0.65 mmHg,第2组为0.39 mmHg(两组之间无统计学差异)。其他血流动力学参数(肺毛细血管楔压、右心室充盈压、心输出量)未发生变化。29%的患者(n = 27)观察到血流动力学“恶化”,定义为Pap升高大于或等于5 mmHg。在这些患者中,低氧血症明显恶化,而其余66例患者未观察到这种情况。(摘要截短于250字)

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